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Stellaria-Studien zur Zytologie, Genetik, Ökologie und Systematik der Gattung Stellaria, insbesondere der Media-Gruppe /Peterson, Daniel, January 1936 (has links)
Thesis (doctoral)--Lunds universitet, 1936. / Reprinted from: Botaniska notiser, 1936. Includes summary in English (p. 413-416). Includes bibliographical references (p. 416-419).
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Polní plevele víceletých pícninKadlček, Leoš January 2017 (has links)
The aim of this diploma thesis is determination of alfalfa (Medicago sativa) infestation in Agricaltural company Kvasicko a. s. The monitoring of infestation was doing from 2013 to 2016 on land Odšenkovna, sawn on 29. 8. 2013, and on land Novina levá, sawn on 11. 4. 2014. Evaluation was made by counting method. The results of this evaluation were processed with DCA analysis and canonical corespondence analysis (CCA). It was found 11 species of weeds on observed lands during the monitoring. The most frequently weeds were: Capsella bursa-pastoris, Stellaria media, Taraxacum sec. Ruderalia and Veronica.
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Molecular authentication of three traditional Chinese medicines: crocodile meat, fish air-bladder and radix stellariae.January 2007 (has links)
Cheung, Chun Wai. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2007. / Includes bibliographical references (leaves 111-128). / Abstracts in English and Chinese. / Acknowledgement --- p.ii / Abstract --- p.iv / 摘要 --- p.vii / Table of content --- p.ix / List of Figures --- p.xvii / List of Tables --- p.xix / Abbreviations --- p.xxi / Chapter Chapter 1. --- Introduction --- p.1 / Chapter 1.1 --- Complementary and Alternative Medicine (CAM) and Traditional Chinese Medicine (TCM) --- p.1 / Chapter 1.2 --- The development of Traditional Chinese Medicine --- p.2 / Chapter 1.3 --- Quality control of Traditional Chinese Medicine --- p.3 / Chapter 1.4 --- Problems of adulteration --- p.5 / Chapter 1.4.1 --- Confusion by common names --- p.5 / Chapter 1.4.2 --- Erroneous and intentional adulteration --- p.6 / Chapter 1.5 --- Authentication of Traditional Chinese Medicine using DNA techniques --- p.7 / Chapter 1.6 --- Crocodile meat --- p.10 / Chapter 1.6.1 --- Crocodile meat as Traditional Chinese Medicine --- p.10 / Chapter 1.6.2 --- Crocodile meat as exotic meat --- p.10 / Chapter 1.6.3 --- Effects of crocodile meat on mice --- p.12 / Chapter 1.6.4 --- Adulteration of crocodile meat in Hong Kong --- p.13 / Chapter 1.6.5 --- Authentication of crocodile meat --- p.14 / Chapter 1.6.5.1 --- SCAR analysis --- p.14 / Chapter 1.6.5.2 --- 12S and 16S ribosomal DNA --- p.14 / Chapter 1.7 --- Fish air-bladder --- p.15 / Chapter 1.7.1 --- Fish air-bladder as Traditional Chinese Medicine --- p.15 / Chapter 1.7.2 --- A case study --- p.16 / Chapter 1.7.3 --- Authentication of fish air-bladder --- p.17 / Chapter 1.8 --- Radix Stellariae --- p.18 / Chapter 1.8.1 --- Stellaria dichotoma L. var. lanceolata Bge --- p.18 / Chapter 1.8.2 --- Radix Stellariae as Traditional Chinese Medicine --- p.19 / Chapter 1.8.3 --- Chemicals in Radix Stellariae and their uses --- p.19 / Chapter 1.8.4 --- Adulteration of Radix Stellariae --- p.20 / Chapter 1.8.5 --- Authentication of Radix Stellariae --- p.21 / Chapter 1.8.5.1 --- Internal Transcribed Spacers (ITS) --- p.21 / Chapter 1.8.5.2 --- trnH-psbA intergenic spacer --- p.23 / Chapter 1.9 --- Objectives --- p.25 / Chapter Chapter 2. --- Materials and Methods --- p.26 / Chapter 2.1 --- Samples used in the study --- p.26 / Chapter 2.1.1 --- Crocodile and monitor lizard samples --- p.26 / Chapter 2.1.2 --- Sequence from NCBI database --- p.26 / Chapter 2.1.3 --- Fish air-bladder samples --- p.30 / Chapter 2.1.4 --- Radix Stellariae samples and samples of related species --- p.33 / Chapter 2.1.5 --- Sequences from NCBI database --- p.33 / Chapter 2.2 --- Reagents and equipments --- p.36 / Chapter 2.2.1 --- Sample preparation and DNA extraction --- p.36 / Chapter 2.2.2 --- Polymerase Chain Reaction --- p.38 / Chapter 2.2.3 --- Agarose gel electrophoresis and Gene Clean --- p.39 / Chapter 2.2.4 --- Cloning --- p.40 / Chapter 2.2.5 --- Cycle sequencing --- p.41 / Chapter 2.3 --- Experimental procedures --- p.42 / Chapter 2.3.1 --- Sample preparation --- p.42 / Chapter 2.3.2 --- DNA extraction --- p.42 / Chapter 2.3.3 --- Polymerase Chain Reaction --- p.44 / Chapter 2.3.4 --- Agarose gel electrophoresis --- p.47 / Chapter 2.3.5 --- Gene Clean --- p.47 / Chapter 2.3.6 --- Cloning --- p.48 / Chapter 2.3.7 --- Cycle sequencing and sequence analyses --- p.51 / Chapter Chapter 3. --- Crocodile meat - Results and Discussion --- p.54 / Chapter 3.1 --- Results --- p.54 / Chapter 3.1.1 --- SCAR analysis --- p.54 / Chapter 3.1.2 --- Sequence analyses --- p.55 / Chapter 3.1.3 --- The dendrograms --- p.56 / Chapter 3.2 --- Discussion --- p.60 / Chapter 3.2.1 --- SCAR as a quick and inexpensive method for the authentication of crocodile meat --- p.60 / Chapter 3.2.2 --- DNA sequencing - A useful tool to identify the source species of the crocodile meat --- p.61 / Chapter 3.2.3 --- Adulteration of crocodile meat in Hong Kong --- p.63 / Chapter 3.2.4 --- Source species of the genuine crocodile meats and the adulterants --- p.63 / Chapter 3.2.5 --- Regulation of labeling of food in Hong Kong --- p.69 / Chapter 3.2.6 --- Source species of the lizard head and tail from AFCD --- p.69 / Chapter 3.3 --- Summary --- p.70 / Chapter Chapter 4. --- Fish air-bladders - Results and Discussion --- p.72 / Chapter 4.1 --- Results --- p.72 / Chapter 4.1.1 --- Identities of sample BH and F1 --- p.73 / Chapter 4.1.2 --- Identity of sample BS --- p.74 / Chapter 4.1.3 --- Identities of samples GD and ZG --- p.74 / Chapter 4.1.4 --- Identity of sample GG --- p.74 / Chapter 4.1.5 --- "Identities of samples HB, HT and SH" --- p.75 / Chapter 4.1.6 --- Identity of sample JL --- p.75 / Chapter 4.1.7 --- Identity of sample MS --- p.76 / Chapter 4.1.8 --- Identity of sample RE --- p.76 / Chapter 4.2 --- Discussion --- p.77 / Chapter 4.2.1 --- Sample RE was confirmed to have originated from rabbit ears --- p.77 / Chapter 4.2.2 --- Identities of the dry fish air-bladders sold in Hong Kong --- p.79 / Chapter 4.2.3 --- Identities of the fresh fish air-bladders sold in Hong Kong --- p.82 / Chapter 4.2.4 --- Limitations of the use of DNA sequences for source species identification --- p.83 / Chapter 4.2.5 --- Variation in prices of fish air-bladders --- p.87 / Chapter 4.3 --- Summary --- p.88 / Chapter Chapter 5. --- Radix Stellariae - Results and Discussion --- p.89 / Chapter 5.1 --- Results --- p.89 / Chapter 5.1.1 --- Sequence analyses --- p.90 / Chapter 5.1.2 --- The dendrograms --- p.90 / Chapter 5.2 --- Discussion --- p.97 / Chapter 5.2.1 --- Identities of the samples obtained from the market --- p.97 / Chapter 5.2.2 --- Identity of sample Sdl4 --- p.97 / Chapter 5.2.3 --- Identities of samples Sd02R and Sd04 --- p.100 / Chapter 5.2.4 --- Myosoton aquaticum in the Stellaria-Myosoton clade --- p.104 / Chapter 5.2.5 --- Medicinal uses of the substitutes of Radix Stellariae --- p.105 / Chapter 5.3 --- Summary --- p.106 / Chapter Chapter 6. --- Conclusion --- p.107 / Reference --- p.111 / Appendix 1. 12S rDNA sequences of crocodilian and Varanus species obtained from NCBI database for sequence analyses --- p.129 / Appendix 2. 16S rDNA sequences of crocodilian and Varanus species obtained from NCBI database for sequence analyses --- p.130 / "Appendix 3. ITS sequences of the species in the genera Arenaria, Myosoton, Silene, and Stellaria obtained from NCBI database for sequence analyses" --- p.131 / Appendix 4. 7rnH-psbA intergenic spacer sequences of Silene species obtained from NCBI database for sequence analyses --- p.132 / Appendix 5. Sequence alignment of 12S rRNA gene sequences of crocodile and monitor lizard samples --- p.133 / Appendix 6. Sequence alignment of 16S rRNA gene sequences of crocodile and lizard samples --- p.141 / Appendix 7. Sequence alignment of coxl sequences of fish air-bladder samples --- p.149 / Appendix 8. Sequence alignment of 12S rRNA gene sequences of fish air-bladder samples --- p.151 / Appendix 9. Sequence alignment of 16S rRNA gene sequences of fish air-bladder samples --- p.153 / Appendix 10. Sequence alignment of coxl region of Vibrio parahaemolyticus and the coxl primers --- p.155 / Appendix 11. Sequence alignment of ITS sequences of Radix Stellariae and related samples --- p.156 / Appendix 12. Sequence alignment of trnH-psbA of Radix Stellariae and related samples --- p.163 / Appendix 13. Search results of coxl sequences of the fish air-bladder samples in BOLD-IDS --- p.167 / Appendix 14. Search results of coxl sequences of the fish air-bladder samples in NCBI nucleotide BLAST --- p.168 / Appendix 15. Search results of 12S rDNA sequences of the fish air-bladder samples in NCBI nucleotide BLAST --- p.169 / Appendix 16. Search results of 16S rDNA sequences of the fish air-bladder samples in NCBI nucleotide BLAST --- p.170 / Appendix 17. Sequence similarities (%) of coxl sequences of the fish air-bladder samples --- p.171 / Appendix 18. Sequence similarities (%) of 12S rDNA sequences of the fish air-bladder samples --- p.172 / Appendix 19. Sequence similarities (%) of 16S rDNA sequences of the fish air-bladder samples --- p.173
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Ekologické determinanty klonálního růstu rostlin / Ecological determinants of plant clonal growthMartincová, Nina January 2016 (has links)
The aim of this study is to provide a further insight into influence of environment on clonal plants. The study focuses particularly on effects of fertilization level and light availability on production and growth of clonal organs. Three experiments were carried out within the study, targeted to elicit influence of these environmental conditions or clonal interactions on six species of clonal plants. Interspecies dependencies on these conditions was compared, regarding habitat occurrence of these species. A comparison was made also between species producing rhizomes and stolons. The experiments revealed that five of six studied species show significant relationship among at least one environmental condition and parameters of clonal reproduction. Most of the species showed higher elongation and production of clonal organs in relation to fertilization level. On the contrary, only three species reacted significantly to the light availability level by alternation of at least one parameter of clonal reproduction and the light availability level affected each species differently. A strong influence on production and elongation of clonal organs had also a size of a plant. There was not found significant difference in influence of environmental conditions on clonal reproduction among plant families. It...
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Effekter av osmotisk potential, samt salteffekter på några vägkantsväxter. / Effects of osmotic potential and salt effects on some roadside plants.Blomqvist, Elin January 2018 (has links)
Syftet med studien var att undersöka effekter på frögroning i form av procentuell frögroning och mean germination time (MGT) för några vanligt förekommande vägkantsväxter till följd av saltning av vägar. Frön från (Prunella vulgaris), getväppling (Anthyllis vulneraria), grått saltgräs (Puccinella distans), grässtjärnblomma (Stellaria graminea) och tjärblomster (Viscaria vulgaris) fördelades i petriskålar och utsattes för mannitol- och natriumkloridlösningar av osmotisk potential -0,3, -0,6 och -0,9 MPa. Mannitol användes för att skilja osmotiska effekter från joniska effekter som natriumklorid ger upphov till. Kontroller med avjoniserat vatten visade frögroning i frånvaro av osmotiska- och joniska effekter. Den procentuella frögroningen var högst i kontrollerna för samtliga arter och minskade med en lägre osmotisk potential. Tjärblomster visade sig gro bäst under samtliga behandlingar. Lägst procentuell groning hade grått saltgräs och grässtjärnblomma. Det tog längre tid för alla arter att gro under en lägre osmotisk potential. Tjärblomster och getväppling visade sig mest känsliga mot abiotiska förändringar och grodde långsammast i förhållande till kontroller för respektive art. Vilket ämne som fröna utsattes för hade ingen påverkan på procentuell groning och MGT, vilket tyder på att det är osmotiska effekter som påverkar arternas frögroning. / The aim of this study was to investigate effects of lowered osmotic potential and osmotic agents on seedling germination and mean germination time (MGT) of some common roadside plants. Seeds of Prunella vulgaris, Anthyllis vulneraria, Puccinella distans, Stellaria graminea and Viscaria vulgaris were distributed in petri dishes and exposed to mannitol and sodium chloride solutions with osmotic potential of -0.3, - 0.6 and -0.9 MPa. Mannitol was used to distinguish osmotic effects from ionic effects caused by sodium chloride. Controls with distilled water showed germination in the absence of osmotic and ionic effects. The percentage of emerged seedlings were highest in controls for all species and decreased with a lower osmotic potential. Viscaria vulgaris had the highest percentage of emerged seedlings across all treatments. The lowest percentage of emerged seedlings had Puccinella distans and Stellaria graminea. It took longer time for all species to germinate under a lower osmotic potential. Viscaria vulgaris and Anthyllis vulneraria turned out to be most sensitive to abiotic changes and grew slowest in relation to controls. There was no difference in the impact of the osmotic agent on percentage germination and MGT, indicating that it is mainly the osmotic effect that affects the seed germination.
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Stable Regimes in an Unstable System: Floral Community and Diversity in the Grand Sable DunesJonathan C Danielson (6622523) 10 June 2019 (has links)
<div>Grand Sable Dunes, as a perched dune field on the shore of Lake Superior, is a sensitive</div><div>ecosystem subject to continual disturbance. Repeated natural disturbances necessitate specialized</div><div>plant communities to develop. There were two objectives of my research in this system that are</div><div>treated in separate chapters. They include: 1) the quantification of successional changes in the</div><div>plant community over time, and the identification of population demography changes for rare</div><div>species within the dunes and 2) the evaluation of evaluate in pollinator species for two plants</div><div>Hieracium caespitosum (Yellow Hawkweed) and Lithospermum caroliniense (Carolina</div><div>Puccoon).</div><div>For the first objective, target plant community composition and structures (i.e. richness,</div><div>diversity) were quantified in 2011 and 2018 across Grand Sable Dunes in 1 m² quadrats.</div><div>Additionally, two relatively rare plant species (Cirsium pitcheri and Tanacetum bipinnatum)</div><div>were selected to quantify demographic (i.e. flowering, non-flowering) patterns and changes over</div><div>time. Samples for C. pitcheri and T. bipinnatum were acquired via circle-plots 2.5 m in diameter.</div><div>Population comparisons between 2011 and 2018 illustrate minimal change in community</div><div>structure (richness and diversity). Composition increased slightly with eight species occurring in</div><div>2018, but not 2011. Additionally, community similarity was high (~78%) between the two years.</div><div>C. pitcheri occurrence was inversely related to presence of other species. Plant community</div><div>composition in eastern and western survey zones within the dunes appear to be diverging. Minor</div><div>changes in the plant community composition and structures indicate successional changes have</div><div>occurred, but without major disturbance. This divergence in community composition may be</div><div>related to weather related incidents associated with Lake Superior disturbance potential.</div><div>The secondary objective concerns pollinator species on two similar plant species found in</div><div>the Grand Sable Dunes. Individuals of H. caespitosum and L. caroliniense were observed and all</div><div>floral visitors were identified to family. The majority of arthropod families were observed</div><div>10</div><div>visiting both H. caespitosum and L. caroliniense, with an absence of typically important families</div><div>(e.g. Apidae, Bombiliidae). Halictidae, Muscidae and Syrphidae were the most common visitors,</div><div>with L. caroliniense attracting far more Muscidae than their H. caespitosum competitors.</div><div>Overlap in visitors for both species was observed, which may lead to decreased reproduction in</div><div>L. caroliniense.</div>
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